rs3098019
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs3098019(G;T) |
Make rs3098019(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 29943495 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs3098019 |
dbSNP (classic) | rs3098019 |
ClinGen | rs3098019 |
ebi | rs3098019 |
HLI | rs3098019 |
Exac | rs3098019 |
Gnomad | rs3098019 |
Varsome | rs3098019 |
LitVar | rs3098019 |
Map | rs3098019 |
PheGenI | rs3098019 |
Biobank | rs3098019 |
1000 genomes | rs3098019 |
hgdp | rs3098019 |
ensembl | rs3098019 |
geneview | rs3098019 |
scholar | rs3098019 |
rs3098019 | |
pharmgkb | rs3098019 |
gwascentral | rs3098019 |
openSNP | rs3098019 |
23andMe | rs3098019 |
SNPshot | rs3098019 |
SNPdbe | rs3098019 |
MSV3d | rs3098019 |
GWAS Ctlg | rs3098019 |
GMAF | 0.1919 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs3098019(A;A) rs3098019(C;C) rs3098019(T;T) |
Alt | rs3098019(A;A) rs3098019(C;C) rs3098019(T;T) |
Reference | Rs3098019(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29911271G>A; NC_000006.11:g.29911271G>C; NC_000006.11:g.29911271G>T |
CLNSRC | |
CLNACC |